JUMP TO CONTENT

Screening Coordinator

JR084686

About the role

This vacancy has now expired. Please click here to view live vacancies.

Job Advert Posting
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.

Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.


-Responsible for undertaking the collation and quality checking procedures of screening source documents and screening test and measurement results within the volunteer screening department and for amending or adding data to the screening source documents as required.
-Be the focal point for screening data queries from within the organization.
-Liaise with the CRC during the preparation of the project start-up and source document design meetings as required.
-Assess and provide to the Recruitment Manager on a daily basis, a review of each project's status in relation to the numbers of subjects available and any outstanding test results.
-Responsible for undertaking all procedures required of the screening data quality checking process.
-Give feedback on a daily basis to staff members assisting with the screening data checking process.
-Be fully conversant with all studies that have been actively recruited for, and ensure relevant staff is informed in a timely manner of any potential panel shortfall, repeat sample requirements, etc.
-Assist with collection and presentation of laboratory results and collated screening data to the designated Physician on a daily basis for medical review and acceptance of subjects for participation in clinical trials.
-Assist with Physician input to determine in a timely manner the completed screening data, a panel of suitable volunteers for each clinical trial.
-Responsible for notifying study-specific recruiter of volunteer status; i.e. selection or DNQ.
-Ensure that the highest levels of ethical and medical confidentially are maintained and that volunteer records are stored securely with restricted access in accordance with the requirements of the HIPAA.
-Responsible for ensuring an accurate and up-to-date volunteer database, including the addition of new volunteers, amendments to detail, notation of contacts, reasons for nonattendance, etc., ensuring a clearly identified volunteer activity audit trail is maintained.
-Be proactive in identifying areas of improvement within the Screening and Recruitment department. Work with peers and management to ensure quality service is provided first time, every time, and where necessary become involved in "Improve" projects to help promote and maintain this philosophy.




Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect the delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfill your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
List #1

Day in the life

Liquid drug vials in palm of hand
Understanding INDs and NDAs in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

04/22/2025

Summary

What is an IND or NDA? A Guide for Aspiring Clinical Research Professionals If you’re considering a career in clinical research or the broader pharmaceutical and biotech industry, you’ve likely c

Teaser label

Discover the difference between IND & NDA applications, and the steps from drug development to regulatory approval.

Read more
Informed consent form
What is an Informed Consent Form (ICF)?

Teaser label

Industry

Content type

Blogs

Publish date

04/22/2025

Summary

When it comes to clinical trials, one of the most important documents you’ll hear about is the Informed Consent Form (ICF). Whether you're starting out in clinical research or exploring job opportunit

Teaser label

Learn what an Informed Consent Form (ICF) is, why it’s essential in clinical research, and how it protects participants.

Read more
Medic in full gown with a clipboard
Clinical Research Associate (CRA) vs Clinical Research Coordinator (CRC)

Teaser label

Industry

Content type

Blogs

Publish date

04/17/2025

Summary

CRA vs CRC Embarking on a career in clinical research is an exciting journey for STEM graduates, offering opportunities to contribute directly to the development of new therapies and to safeguard

Teaser label

Discover the key differences between Clinical Research Associates (CRA) and Clinical Research Coordinators (CRC).

Read more
View all

Similar jobs at ICON

Clinical Research Associate II/ Senior Clinical Research Associate

Salary

Location

Brisbane

Department

Clinical Monitoring

Location

Brisbane

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Clinical Research Associate/ Senior Clinical Research AssociateLocation: Home-based in Brisbane ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to f

Reference

2025-119092

Expiry date

01/01/0001

Krisztina Auth Read more Shortlist Save this role
Optometrist

Salary

Location

Johns Creek

Department

Regulatory, Drug Safety/ Quality Assurance & Other roles

Location

Johns Creek

Remote Working

Office Based

Business Area

ICON Strategic Solutions

Job Categories

Laboratory

Job Type

Permanent

Description

As a Optometrist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This position is located in Johns Creek, GA.

Reference

2025-118910

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
Global Senior Study Site Specialist

Salary

Location

Canada

Department

Study Start Up

Location

Canada

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Study Start Up

Job Type

Permanent

Description

Under the guidance of the Director of Global Site Management & Central Services, this position will be responsible for conducting end-to-end site management from feasibility to site activation serving

Reference

2025-117897

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Project Manager II, Laboratory

Salary

Location

US, Farmingdale, NY

Department

Full Service - Development & Commercialisation Solutions

Location

New York

Blue Bell

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Project Management

Project Management

Job Type

Permanent

Description

Project Manager II, Laboratory- Blue Bell PA or Farmingdale NY- hybrid The Project Manager, Labs will ensure client satisfaction by acting as the Client's main contact in all matters regarding ICON La

Reference

JR129968

Expiry date

01/01/0001

Frank Lampart

Author

Frank Lampart
Read more Shortlist Save this role
Senior Project Manager, Laboratory

Salary

Location

US, Farmingdale, NY

Department

Full Service - Development & Commercialisation Solutions

Location

New York

Blue Bell

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Project Management

Project Management

Job Type

Permanent

Description

Senior Project Manager, Laboratory- Location: Farmingdale NY or Blue Bell, PA- That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us.

Reference

JR129615

Expiry date

01/01/0001

Frank Lampart

Author

Frank Lampart
Read more Shortlist Save this role
Senior Manager, Regulatory Affairs Advertising and Promotion

Salary

Location

United States

Department

Regulatory, Drug Safety/ Quality Assurance & Other roles

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Regulatory Affairs

Job Type

Permanent

Description

The Asspcoate Dirctor, Regulatory Affairs Advertising & Promotion will be responsible for providing strategic, operational and tactical regulatory advice to internal stakeholders regarding communicati

Reference

2025-117935

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above